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Volumn 13, Issue 6, 2005, Pages 1969-1975
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2,7-Dihydro-3H-pyridazino[5,4,3-kl]acridin-3-one derivatives, novel type of cytotoxic agents active on multidrug-resistant cell lines. Synthesis and biological evaluation
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Author keywords
Acridine analogs; Antitumor compounds; Cytotoxic activity; Multidrug resistance
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Indexed keywords
2 (2 MORPHOLINOETHYL) 2,7 DIHYDRO 3H PYRIDAZINO[5,4,3 KL]ACRIDIN 3 ONE;
2 (2 PIPERIDINOETHYL) 2,7 DIHYDRO 3H PYRIDAZINO[5,4,3 KL]ACRIDIN 3 ONE;
2 [2 (DIMETHYLAMINO)ETHYL] 2,7 DIHYDRO 3H PYRIDAZINO[5,4,3 KL]ACRIDIN 3 ONE;
2 [3 (DIMETHYLAMINO)ETHYL] 2,7 DIHYDRO 3H PYRIDAZINO[5,4,3 KL]ACRIDIN 3 ONE;
2 [3 (DIMETHYLAMINO)PROPYL] 2,7 DIHYDRO 3H PYRIDAZINO[5,4,3 KL]ACRIDIN 3 ONE;
6 CHLORO 2 [2 (DIMETHYLAMINO)ETHYL] 2,7 DIHYDRO 3H DIBENZO[DE,H]CINNOLINE 3,7 DIONE;
6 CHLORO 2 [2 (DIMETHYLAMINO)PROPYL) 2,7 DIHYDRO 3H PYRIDAZINO[5,4,3 KL]ACRIDIN 3 ONE;
6 CHLORO 2,7 DIHYDRO 3H PYRIDAZINO[5,4,3 KL]ACRIDIN 3 ONE;
9 OXO 9,10 DIHYDROACRIDINE 1 CARBOXYLATE;
ACRIDINE DERIVATIVE;
CYTOTOXIC AGENT;
DOXORUBICIN;
HYDRAZINE DERIVATIVE;
MITOXANTRONE;
MULTIDRUG RESISTANCE PROTEIN;
PHOSPHORUS DERIVATIVE;
PYRIDAZINONE DERIVATIVE;
UNCLASSIFIED DRUG;
VINCRISTINE;
ANIMAL CELL;
ARTICLE;
CONTROLLED STUDY;
CYTOTOXICITY;
DRUG DNA BINDING;
DRUG SCREENING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
LEUKEMIA CELL;
LYMPHATIC LEUKEMIA;
MULTIDRUG RESISTANCE;
MYELOID LEUKEMIA;
NONHUMAN;
PROMYELOCYTIC LEUKEMIA;
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EID: 13844305773
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2005.01.023 Document Type: Article |
Times cited : (27)
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References (17)
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